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Work closely with the Head of Scientific Affairs & Strategic Partnerships and Scientific Affairs team to produce rapid, thoughtful responses to content-related requests from across Pfizer Oncology (CSO, Medical strategy, BoD, Investor Relations, colleagues, etc.
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4 years of managed care experience required, preferably in regulatory affairs/compliance. Position Overview Reporting to the Senior Manager of Medicare Regulatory Compliance, the Medicare Regulatory Compliance Specialist will support the oversight and management of the Medicare Compliance Program.
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Job Overview: The Derivatives Associate Attorney will provide legal support in transactional and regulatory matters related to derivatives trading. Strong understanding of derivatives trading and related regulatory frameworks.
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Leads all human capital management functions including talent management (recruiting, performance management, training); compensation and benefits; human resources information systems; civil service; labor relations (collective bargaining and administration of all collective bargaining agreements); and regulatory requirements (in conjunction with Legal Department.
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Position Title: Director for Major Gifts and Parent Fundraising Position Number: 896631 School/Division: Office of Vice Pres. of Development (division) Full-Time or Part-Time: Full-Time Description: Reporting to the Senior Vice President for Development and Alumni Affairs, the Director of Major Gifts and Parent Fundraising will be a strategic leader within the University’s Development Office.
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The Moody’s Analytics (MA) Risk Management team within the Customer, Operations, and Risk group oversees MA’s enterprise risk management framework and implements its risk management activities, with the objectives of safeguarding sensitive business data, protecting data privacy, addressing information security threats, ensuring legal and regulatory compliance, meeting customer requirements for controls assurance, and promoting risk awareness.
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Ensure compliance with IRC procurement policies and procedures, regulatory requirements and industry and donor standards for the procurement of medical, nutrition, WASH and NFI commodities Cultivate and maintain strong relationships with vendors and internal requestors, particularly Pharma/Health Technical Advisors, fostering teamwork and resolving issues promptly.
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Keeps abreast and knowledgeable about ongoing and emerging Infection Prevention and Control topics, regulatory requirements, and quality and reporting metrics as determined by CHE Trinity, the Joint Commission on Accreditation of Healthcare Organizations, the Centers for Medicare and Medicaid Services, the Centers for Disease Control and Prevention, local, state, and national health departments.
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Collaborate closely with cross-functional teams, including Clinical Development, Commercial, Regulatory, and Medical Affairs, to drive the success of our product. Position Overview:We are seeking a dynamic and experienced Senior Director, Field Medical Affairs to join an innovative team at a highly reputable clinical-stage biopharma headquartered in Princeton, NJ.
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Responsibilities & Qualifications Preparation of construction documents in AutoCAD. Proficient in Civil 3D Experience / Knowledge in Microstation is a plus Remaining up to date on regulatory agency standards, and review procedures.
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Mizuho has in place a hybrid working program, with varying opportunities for remote work depending on the nature of the role, needs of your department, as well as local laws and regulatory obligations.
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Axsome Therapeutics is seeking an Associate Director/Director, Regulatory Affairs Advertising & Promotion to The Associate Director/Director, Regulatory Affairs Advertising & Promotion will help to establish and implement the promotional regulatory strategy for the company and will work with the Executive Director, Regulatory Affairs Advertising and Promotion to ensure professional and efficient interactions between the company and Office of Prescription Drug Promotion (OPDP.
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Ensure compliance with both PSEGLI Policies and Procedures and applicable regulatory agencies. Our focus on combatting climate change through clean energy technology, our new net zero climate vision for 2030 and enhanced commitment to diversity, equity and inclusion; and supporting the communities we serve make this a particularly exciting time to join PSEG.
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IT Audit ExperienceFinancial Services experienceUnderstanding of Regulatory AssessmentsFamiliar with IT Risk Management FrameworksProficiency in advanced Excel and other reporting tools. Our client, an enterprise financial services organization, is looking to hire an experienced Audit and Regulatory professional within their Global Cyber Security's Risk Product Management team.
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12+ years of relevant compliance and regulatory experience in finance, fintech, or crypto exchanges (experience in AML/BSA compliance is a must) We look for those who possess sound judgment, curiosity, and are able to adapt to a changing regulatory digital asset landscape.
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regulatory affairs jobs Title: sr director Company: Planet Pharma in East Meadow, NY
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